GUDIDData
eudamed_udi Primary ID: +G590SD30TP3505

SD30T P3,5 (UDI +G590SD30TP3505)

Manufactured by IDETEC SAS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SD30T P3,5 - Primary ID +G590SD30TP3505

Device Regulatory Overview

The SD30T P3,5 (Model/Catalog Number: SD30T P3,5) is a medical device manufactured by IDETEC SAS. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SD30T P3,5
Product Code / EMDN
Z11039016
Device Name
Mobile Radiographic Units & C-arm - Radiographic/Fluoroscopic Units
Database Sync Date
2026-08-09 16:46:14

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of SD30T P3,5?

The registered manufacturer of record for SD30T P3,5 is IDETEC SAS.

What is the Primary UDI-DI identifier for SD30T P3,5?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G590SD30TP3505.

What classification code is assigned to this device?

This device is registered under product classification code Z11039016.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint